E L F HOLY HYDRATION FACE SPF 30 SUNSCREEN,- avobenzone, homosalate, octisalate, octocrylene cream

e l f Holy Hydration Face SPF 30 Sunscreen, by

Drug Labeling and Warnings

e l f Holy Hydration Face SPF 30 Sunscreen, by is a Otc medication manufactured, distributed, or labeled by e.l.f. Cosmetics, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Avobenzone 3.0%

Homosalate 7.3%

Octisalate 4.0%

Octocrylene 8.5%

Purpose

Sunscreen

Use

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only.

Do not use

on damaged or broken skin.

When using this product:

Keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if:

rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Other Information

• Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours.
• Use water resistant sunscreen if swimming or sweating.
• Sun Protection Measures:Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in sun, especially from 10 a.m.-2 p.m., wear long-sleeved shirts, pants, hats and sunglasses. Children under 6 months of age: ask a doctor.

Other Information

• Protect the product in this container from excessive heat and direct sun.

Inactive Ingredients

Water (Aqua), Glycerin, Polyglyceryl-3 Distearate, Niacinamide, Aluminum Starch Octenylsuccinate, Trehalose, Stearyl Heptanoate, Silica, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Panthenol, Sodium Hyaluronate, Squalane, Butylene Glycol, Caprylyl Glycol, Ethylhexylglycerin, Stearic Acid, Palmitic Acid, Cetearyl Olivate, Sorbitan Olivate, Cetearyl Alcohol, Glyceryl Stearate Citrate, Dimethicone, Polyacrylate-13, Polyisobutene, Polysorbate 20, Sorbitan Isostearate, Carbomer, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Disodium EDTA, Phenoxyethanol, Fragrance(Parfum), Geraniol, Linalool

Questions or comments?

1-888-315-9814

Package Labelling;

INGREDIENTS AND APPEARANCE

E L F HOLY HYDRATION FACE SPF 30 SUNSCREEN, 
avobenzone, homosalate, octisalate, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76354-447
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	73 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	40 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	85 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
NIACINAMIDE (UNII: 25X51I8RD4)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
TREHALOSE (UNII: B8WCK70T7I)
STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
PANTHENOL (UNII: WV9CM0O67Z)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SQUALANE (UNII: GW89575KF9)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYACRYLATE-13 (UNII: FS2D4T67EA)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GERANIOL (UNII: L837108USY)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76354-447-01	50 g in 1 TUBE; Type 0: Not a Combination Product	07/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/20/2024

Labeler - e.l.f. Cosmetics, Inc (093902816)